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Natural Killer Cells Reconstitution Kinetics Post Haploidentical Transplantation

Natural Killer Cells Reconstitution Kinetics Post T Cells Repleted Haploidentical Transplantation

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02978274
Enrollment
200
Registered
2016-11-30
Start date
2015-03-31
Completion date
2022-12-31
Last updated
2020-10-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Natural Killer Cell Mediated Immunity

Brief summary

Patients undergoing haploidentical allo-HSCT will be prospectively enrolled exploring the NK cells phenotype and functional reconstitution.

Detailed description

Patients with hematological malignancies suitable for allo-HSCT but without HLA-identical related or unrelated donors were candidates for the HLA-haploidentical HSCT. Patients undergoing haploidentical allo-HSCT will be prospectively enrolled exploring the NK cells phenotype and functional reconstitution. Peripheral blood will be collected by day15, 30, 60, 90, 180, and 1 year post transplantation.

Interventions

DRUGMMF

MMF withdrawal by engraftment post haplo-SCT

Sponsors

Peking University People's Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
15 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* AML or MDS or CML or ALL undergoing haploidentical stem cells transplantation

Exclusion criteria

* NR or refractory AML/ALL before transplantation donors from mother or collateral related

Design outcomes

Primary

MeasureTime frame
Immune Reconstitution differences between two group1 year

Secondary

MeasureTime frame
Cumulative incidence of acute GVHD differences between two group100 day
Cumulative incidence of chronic GVHD differences between two group1 year
Cumulative incidence of TRM differences between two group1 year
Cumulative incidence of Infection differences between two group1 year
DFS differences between two group1 year
OS differences between two group1 year
Cumulative incidence of relapse differences between two group1 year

Countries

China

Contacts

Primary ContactXiangyu Zhao, M.D., PhD
xyz80421@126.com+8610-88325949

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 21, 2026